Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors with
heterogeneous clinical presentations and potential lethal outcomes. The diagnosis is based …

Introduction Pheochromocytoma is a tumour arising from the adrenal medulla, which
secretes catecholamines. Approximately 20% of pheochromocytomas are cystic and more …

Conclusion: Giant pheochromocytoma is an uncommon neoplasm. It can be discovered late
due to a lack of clinical manifestations. Diagnosis is dependent on imaging recognition …

Pheochromocytomas are tumors that develop from the chromaffin cells of the adrenal
medulla. More than 40% of cases of pheochromocytomas are associated with genetic …

Introduction Pheochromocytoma is a neuroendocrine tumor originating from chromaffin cells
in the adrenal medulla. Giant pheochromocytomas with a maximum diameter of over 20 cm …

Cystic PPGL is rare, and clinical manifestations are often atypical. Clinicians have
conducted more frequently diagnostic screenings for adrenal cystic mass due to the …

Introduction Since pheochromocytomas present with various complications due to
catecholamine hypersecretion, their perioperative management needs special attention …

Pheochromocytomas are rare tumors arising from chromaffin cells of the adrenal medulla
and extramedullary sympathetic ganglia. The incidence of asymptomatic disease is rising …

The article present a case study of a 50-year-old female with weakness and nausea with
dyspepsia on and off since the last 3 months. It mentions computed tomography (CT) scan …

Pheochromocytomas are neuroendocrine tumors that arise from chromaffin cells in the
adrenal medulla. Giant pheochromocytomas commonly measure greater than 7 to 10 cm …